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Dynamic NMR studies of ferrocenylsulphide-palladium(II) and -platinum(II) complexes
Authors:Keith G. Orrell  Vladimir Šik  Carl H. Brubaker  Beth McCulloch
Affiliation:Department of Chemistry, The University, Exeter, EX4 4QD Great Britain;Department of Chemistry, College of Natural Science, Michigan State University, East Lansing, Michigan 48824 U.S.A.
Abstract:The stereodynamics of ferrocenylsulphide-palladium(II) and -platinum(II) complexes, Fe(C5H4SR)2MX2, (M = PdII, PtII; X = Cl, Br; R = Ph, i-Pr and i-Bu), have been examined by variable temperature NMR. At temperatures down to ca. ?100° C, the pyramidal inversion of the S atoms could be slowed down sufficiently to yield accurate energy data, while the reversal of the ferrocenophane ring remained fast on the NMR time scale. ΔG data for the S inversion process were in the range 47 to 65 kJ mol?1 and were influenced to varying extents by the nature of the transition metal, the halogen, and the R substituent on the sulphur.
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